Productos Mayaland, SA de CV
FDA import alert and refusal historyValladolid, MexicoFEI 3017708840
As of October 26, 2026, Productos Mayaland, SA de CV is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 22, 2022, most often for substitute (SUBSTITUTE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Honey · SUBSTITUTE
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Productos Mayaland, SA de CV
2 records, newest first. Each line links to the FDA page it came from.
2024
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2022
- Import refusalRefused, HoneySUBSTITUTEEntry AC1-6524513-8Source
Refusal charges, in plain English
- SUBSTITUTE1 refused line
SUBSTITUTE
Questions about Productos Mayaland, SA de CV
- Is Productos Mayaland, SA de CV on an FDA import alert?
- No listing for Productos Mayaland, SA de CV appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
- Has FDA refused shipments from Productos Mayaland, SA de CV?
- Yes. FDA refused 1 shipment line from Productos Mayaland, SA de CV on November 22, 2022. The most recent, on November 22, 2022, was honey, charged as SUBSTITUTE (substitute).
- Why did FDA refuse Productos Mayaland, SA de CV's shipments?
- The most frequent charge is SUBSTITUTE (substitute, 1 line).
- When was Productos Mayaland, SA de CV last inspected by FDA?
- FDA's most recent inspection of Productos Mayaland, SA de CV with a final classification is dated August 7, 2024 and was classified VAI (Voluntary Action Indicated).
- What is Productos Mayaland, SA de CV's FEI number?
- Productos Mayaland, SA de CV's FDA Establishment Identifier (FEI) is 3017708840.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.